A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603863



Internal ID6990894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3818631..3825583hg38UCSC Ensembl
Innerchr5:3818657..3825557hg38UCSC Ensembl
Outerchr5:3818605..3825609hg38UCSC Ensembl
chr5:3818745..3825697hg19UCSC Ensembl
Innerchr5:3818771..3825671hg19UCSC Ensembl
Outerchr5:3818719..3825723hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg386953
hg196953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11791621
SamplesHG03757
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603863
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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